The development of salmon, Salmo salar L., ranching in Iceland, with a special reference to homing and recapture techniques

Abstract. The paper describes the development and current status of salmon, Salmo salar L., ranching in Iceland, with a special emphasis on recapture techniques and homing to the release sites. Many ranching operations are located at release sites with little or no rearing activity except for a short acclimatization period before release. This technique was a breakthrough in Icelandic ranching development, as most suitable ranching sites do not have suitable conditions for smolt rearing. Ranching is mostly practised on the west coast of Iceland, where ranched salmon made up over 80% of the total catch in 1991. The largest ranching stations are Kollafjördur and Vogavík in south-western Iceland and two stations, Lárós and Silfurlax, located on the outer part of Snæfellsnes. Combined releases in 1991 were about 6 million smolts and 130 thousand salmon were harvested from ranching. Ranched salmon are mostly harvested from June to August with a peak run in July. The methods of recapture vary considerably. At Kollafjördur Fish Farm, which has river water for attraction, the salmon are mostly caught in riverine traps of conventional design, but during periods of draught an estuarine seining process has been practised to secure bright salmon. At Vogavík, which only has pumped well water for attraction, catches have been based on efficient estuarine traps. Similar methods have been used at the Silfurlax operation in Hraunsfjördur. Homing to ranching sites has been shown to be fairly precise, especially if smolts are released in fresh water and suitable ranching stocks are used. There are indications that the Kollafjördur ranching strain, which has been developed over a period of 25 years, has better homing than wild stocks. Considerable straying has been observed, primarily between ranching stations and into the outflows of large land-based salmon farms. Straying into salmon streams seems to vary from year to year and is greatest in the vicinity of large ranching stations. It seems to occur in late summer, possibly as a result of inadequate recapture techniques at the ranching sites.     

High marine survival rates of sea‐ranched Atlantic salmon smolts (Salmo salar) that had previously matured as male parr

Abstract The growth and recapture rates of Atlantic salmon, Salmo salar L., smolts that had previously matured as parr were compared with those of immature siblings in a sea‐ranching experiment in western Norway. The smolts were the offspring of three river populations. They were individually tagged, transferred to cages in a small bay where estuarine salinity gradients had been established and released on four dates from mid‐May to early June after either 3 or 7 days of acclimatisation. The previously mature male parr (PMMP) were smaller than their siblings before release, but performed much better during their time in the sea. As grilse, they reached sizes comparable with the formerly immature fish, and their recapture rate was more than four times higher (8.6 vs 2.1%). This difference decreased somewhat during the following years because 0.85% of the immature fish and only 0.1% of PMMP were recaptured as multi‐sea‐winter salmon. The highly successful marine performance of the PMMP demonstrated that this life history strategy may be more flexible than previously believed.     

Straying of Atlantic salmon, Salmo salar, from delayed and coastal releases in the Baltic Sea, with special focus on the Swedish west coast

Abstract  Atlantic salmon, Salmo salar L., reared from two Baltic strains were released around the islands Bornholm and Møn in the Baltic Sea between 1995 and 1999. A total 600 000 reared salmon were released from net pens using the delayed release technique, keeping the salmon in net pens for approximately 3 months after smolting, and 208 000 were released directly from the hatchery. Of these, 15 958 were tagged with Carlin tags. Additionally, 65 300 coded wire tagged salmon were released as delayed release salmon close to Bornholm in 2000. Recaptures from the five years of Carlin tagged releases varied between 2.8% and 21.2% (average 13.1%). Most recaptures were from within the Baltic Sea (average 98%), but some were recaptured outside the Baltic Sea, either in the sea (1%) or in fresh water (1%). Recaptures outside the Baltic Sea and in fresh water were higher for releases at Møn in the western part of the Baltic, than releases at Bornholm. Straying rates from the releases into six rivers on the Swedish west coast were estimated using information from capture in traps and sport and broodstock fisheries. The proportion of straying salmon in rivers on the Swedish west coast was about 3.8% of the salmon run, but with large variations between rivers. Releases were discontinued because of possible deleterious effect on the local wild salmon populations.     

Atlantic salmon smolts in the Irish Sea: First evidence of a northerly migration trajectory

Results from an acoustic telemetry study revealed for the first time a northerly migration route for Atlantic salmon (Salmo salar L.) smolts leaving the east coast of Ireland. Atlantic salmon smolts were tagged in spring 2019 in the Castletown and Boyne rivers. Three tagged smolts registered on disparate deep‐water offshore marine receivers as they travelled northwards out of the Irish Sea through the North Channel. One fish had migrated an estimated 250 km in a period of 32 days. The remaining two individuals were detected on receivers located off the Northern Ireland coast, further corroborating the northward migration of salmon smolts through the Irish Sea.     

Strontium levels in scales and vertebrae of wild and hatchery-reared Atlantic salmon, Salmo solar L., smolts

Abstract. Analyses of the Sr-contenl in scales of Atlantic salmon, Salmo saiar L ., smolts from two hatcheries revealed significant ( P < 0·001) differences. These differences were reflected in the Sr-conients of their respective diets. Sr-values in scale samples taken from wild salmon smolts from 10 Norwegian rivers showed a considerable variation. Analysis of variance showed that sampling site was the major source of variation. In general the Sr-content in scales cannot be used to distinguish between hatchery-reared and wild salmon smolls, although the present results nevertheless suggest that such a distinction is possible in some localities.
The Sr-contenl of the vertebrae was somewhat lower than that of the scales in both hatchery-reared and wild smolls. The Sr-conient of the scales of sea trout, Salmo trutta L., smolts from one of the sampling sites was significantly ( P < 0·001) higher than that of scales of Atlantic salmon smolts from the same site. The Sr-content of the scales of all the salmon smolts sampled from a lake was higher than the values recorded for sea trout and salmon after their stay in the sea. Use of the Sr-contenl of the scales todistinguish between migratory and resident individuals should therefore be done with care.     

Sea lice, Lepeophtheirus salmonis, transfer between wild sympatric adult and juvenile salmon on the north coast of British Columbia, Canada

We examine sea lice, Lepeophtheirus salmonis , on juvenile and adult salmon from the north coast of British Columbia between 2004 and 2006 in an area that does not at present contain salmon farms. There is a pronounced zonation in the abundance of L. salmonis on juvenile pink salmon, Oncorhynchus gorbuscha , in the Skeena and Nass estuaries. Abundances in the proximal and distal zones of these estuaries are 0.01 and 0.05 respectively. The outer zones serve as feeding and staging areas for the pink salmon smolts. Returning Chinook, Oncorhynchus tshawytscha , and coho salmon, Oncorhynchus kisutch , concentrate in these areas. We collected data in 2006 to examine whether L. salmonis on returning adult salmon are an important source of the sea lice that appear on juvenile pink salmon. Nearly all (99%) of the sea lice on returning Chinook and over 80% on coho salmon were L. salmonis. Most of the L. salmonis were motile stages including many ovigerous females. There was a sharp increase in the abundance of sea lice on juvenile pink salmon smolts between May and July 2006 near the sites of adult captures. As there are no salmon farms on the north coast, few sticklebacks, Gasterosteus aculeatus , and very few resident salmonids until later in the summer, it seems that the most important reservoir of L. salmonis under natural conditions is returning adult salmon. This natural source of sea lice results in levels of abundance that are one or two orders of magnitude lower than those observed on juvenile pink salmon in areas with salmon farms such as the Broughton Archipelago.     

Diel migration pattern of Atlantic salmon (Salmo salar) and sea trout (Salmo trutta) smolts: an assessment of environmental cues

The timing of smolt migration is a key phenological trait with profound implications for individual survival during both river descent and the subsequent sea sojourn of anadromous fish. We studied relationships between the time of smolt migration, water temperature and light intensity for Atlantic salmon (Salmo salar) and sea trout (Salmo trutta). During 2006–2012, migrating smolts descending the southern Norway River Storelva were caught in a rotary screw trap located at the river mouth. The date of 50% cumulative smolt descent correlated significantly with the date when the river temperature exceeded 8°C for both Atlantic salmon and sea trout smolts. In 2010, smolts of both species were passive integrated transponder (PIT)‐tagged, and the diel timing of their migration was precisely documented. The degree of night migration decreased in both species as the river temperature rose, and at temperatures above 12–13°C, more smolts migrated during day than during night. A multinomial model was fitted for estimating temperature and species effects on probabilities of migration during night, daytime, dusk and dawn. Atlantic salmon smolts preferred migrating under lower light intensities than sea trout smolts during early, but not late spring when both species migrated during bright daylight. In accordance with the early‐season tendency to migrate at night, Atlantic salmon smolts migrated more during darker hours of the day than sea trout. In both species, smaller smolts migrated under dark conditions than during light conditions. Most of the findings on thermal, light and temporal effects on the observed smolt migration pattern can be explained as adaptations to predation avoidance.     

Marine temperatures experienced by postsmolts and the survival of Atlantic salmon, Salmo salar L., in the North Sea area

The survival of two Atlantic salmon stocks that inhabit rivers confluent with the North Sea was examined in respect to historical distributions of sea surface water temperatures. The rivers Figgjo and North Esk are relatively small salmon rivers in southern Norway and eastern Scotland, respectively. Wild salmon smolts have been tagged in these rivers since 1965. Tag returns were used to evaluate the survival of salmon in the North Sea. Survival rates of one-sea-winter (1SW) and 2SW fish were correlated within stocks, as well as between stocks. Survival rates were compared with the areal extent of thermal habitat in the north-eastern Atlantic Ocean. A positive correlation was found between the area of 8–10°C water in May and the survival of salmon. A reciprocal negative correlation was also found between survival and 5–7°C water in the same month. An analysis of sea surface temperature distributions for periods of good vs. poor salmon survival showed that when cool surface waters dominate the Norwegian coast and North Sea during May, salmon survival has been poor. Conversely, when the 8°C isotherm has extended northward along the Norwegian coast during May, survival has been good. The effect of water temperature distributions on the growth of postsmolts and other survival factors are discussed.     

Relationship between sea lice levels on sea trout and fish farm activity in western Scotland

The relationship between aquaculture and infestations of sea lice on sea trout, Salmo trutta L., is controversial. Here, the association between sea lice infestations on wild sea trout and characteristics of local Atlantic salmon, Salmo salar L., farms were investigated using data collected on the Scottish west coast. The proportion of sea trout with louse burdens above a critical level was positively related to the fork length of the sea trout and the mean weight of salmon on the nearest fish farm, and negatively related to the distance to that farm. The distance to the nearest fish farm did not influence the probability of infestations above the critical level beyond 31 km although there was considerable uncertainty around this cut‐off distance (95% limits: 13–149 km). The results support a link between Atlantic salmon farms and sea lice burdens on sea trout in the west of Scotland and provide the type of information required for marine spatial planning.     

Differences in sea migration between wild and reared Atlantic salmon (Salmo salar L.) in the Baltic Sea

The effect of origin, smolt size and year of release on the sea migration pattern of Atlantic salmon (Salmo salar L.) in the Baltic Sea was examined by tagging experiments conducted in 1991–1993 on wild and reared smolts of the Simojoki river salmon stock. The tag recovery data analysed by log-linear models revealed significant differences in both spatial and temporal sea migrations between the wild and reared salmon; the variation was attributed to the year of release and to the origin of the fish. Grilse accounted for the majority of reared returners (76%) but for a smaller proportion (46%) of the wild fish. The effect of smolt size could be studied only in the smolt groups tagged in 1991. Wild fish were more frequently (71%) caught in the Baltic Main Basin than were reared fish (51%) during their second sea year, and the size variation between wild and reared smolts did not explain the recovery site. No such differences in spatial distribution were found during the third sea year. The tagging place (hatchery/trap) of the reared fish did not affect their later sea migration. The differences in sea migration patterns suggest that the wild salmon are more vulnerable to the intensive salmon fishery in the Baltic Main Basin than are reared fish.     

Movements of two strains of radio tagged Altlantic salmon, Salmo salar L., smolts through a reservoir

Smolt migration through a shallow and turbid hydro-reservoir in a major Danish river system was investigated using radiotelemetry. Hatchery-reared 1+-year-old Atlantic salmon, Salmo salar L., smolts of equal size from two different non-native strains were radio-tagged and followed during their downstream migration through the 12-km-long reservoir. A total of 50 salmon smolts, 25 of Swedish (Øtran River) and 25 of Irish (Burrishoole River) origin, were surgically implanted with miniature radiotransmitters. The tagged smolts were tracked daily over a 3-week period in May 1996. The Øtran smolts initiated migration first ( P  < 0.001), moved faster ( P  < 0.01), were delayed less when passing a culvert ( P  < 0.001) and were more successful in moving through the reservoir than the Burrishoole smolts. The observed differences in migratory behaviour are interpreted as evidence of a genetic component influencing smolt migration.     

Linking habitat characteristics with juvenile density to quantify Salmo salar and Salmo trutta smolt production in the river Sävarån,Sweden

Abstract Habitat mapping along 85 km of river was related to juvenile (15 years of electric fishing) and smolt (3 years of screw‐trapping) abundance data to estimate salmon, Salmo salar L., and sea trout, Salmo trutta L., smolt production in the River Sävarån, northern Sweden. Spawning site selection by radio‐tagged salmon (n = 12) and sea trout (n = 4) was also assessed. Fifty‐one hectares of potential spawning and nursery habitat was found in the main stem river, representing 25% of the total river area. These areas were estimated to yield 1300–7580 salmon and 630–3540 sea trout smolts based on juvenile densities, equating with 3 years of screw‐trap data (2990–5080 salmon and 680–2520 trout smolts, respectively). A hypothetical maximum production of about 19 900 salmon smolts was predicted for the river at a density of 40, 0+ salmon 100 m^?2. Tracking adults during the spawning period identified optimal and potential reproductive areas.     

Comparison of growth rate in Atlantic salmon,pink salmon,Arctic char,sea trout and rainbow trout under Norwegian farming conditions

Growth rates of Atlantic salmon, pink salmon, Arctic char, sea trout and rainbow trout were compared under Norwegian farming conditions. During the juvenile, freshwater period, growth was fastest in pink salmon, followed by rainbow trout and Arctic char. Freshwater growth of sea trout and, especially, Atlantic salmon, was slow. After transfer of smolts or fingerling to sea water, Arctic char failed to survive the autumn. Sea water growth of sea trout was slow, but the three species, rainbow trout, Atlantic salmon and pink salmon, all grew rapidly through all seasons. When in sea water, rainbow trout and pink salmon were regularly attacked by vibriosis, while Atlantic salmon were rarely attacked, and sea trout never. It is concluded that, for commercial farming in Norway, rainbow trout are of value for production of fish of any size up to 3–4 kg, and pink salmon for production of small fish of 0.5–1.5 kg. Atlantic salmon is the only species suitable for production of a very large salmonid, i.e., more than 4–5 kg.     

Effects of the Faroese long-line fishery, other oceanic fisheries and oceanic variations on age at maturity of Icelandic north-coast stocks of Atlantic salmon (Salmo salar)

Investigations were conducted on the effects of oceanic variations (as indicated by sea temperatures) and catches of the Faroese, Norwegian Sea and West Greenland salmon fisheries on the sea-age composition of Atlantic salmon (Salmo salar L.) from 22 Icelandic north-coast rivers. Catches of grilse in rivers were strongly correlated among the 22 rivers, as were the ratios of grilse caught to two-sea winter (2SW) salmon caught the next year. Four of the 22 rivers showed increasing ratios over time and three of these rivers, all in the northeast, had significantly higher mean ratios after the expansion of the Faroese fishery than before (P < 0.05). No evidence was found from ratios for the other 18 rivers to suggest that Faroese fishing was significantly depleting those stocks, even though 13 micro-tagged north-coast salmon had been recovered in the fishery in the 1988–1989 season. No evidence was found that Norwegian Sea or West Greenland fisheries affected stock composition. The mean April–May sea temperature prior to when the smolts enter the sea was significantly and positively related to ratios in eight of the 22 rivers. This result, along with frequent significant correlations in ratios among rivers, indicated that more rapid growth of smolts in their first summer may have increased grilse to 2SW salmon ratios on several rivers.     

Relationships between marine growth and marine survival of one sea winter Atlantic salmon, Salmo salar L., from the River Bush, Northern Ireland

An examination of marine growth/marine survival relationships in Atlantic salmon, Salmo salar L., was carried out, based on scale growth measurements in relation to two indices of marine survival in wild fish from the River Bush, Northern Ireland. The survival of cohorts to the Irish/Northern Irish coast (prefishery) and to fresh water was statistically unrelated to variation in growth from smolt migration to the end of the first winter at sea ( P  > 0.1; – P  > 0.7). Marine growth of 1+ smolts decreased significantly during the period of the study ( P  < 0.05), but growth of 2+ smolts did not change ( P  > 0.05). The variability in marine growth was much less than the variation in natural survival at sea, suggesting that factors instead of or in addition to, growth influence natural survival in the marine environment. Survival to fresh water was not related to survival to the coast ( P  > 0.4), although it was inversely correlated with exploitation rate ( P  < 0.01). These results are discussed in relation to the use of freshwater returns to assess marine survival and the potential for the variation in natural marine mortality to influence total life-cycle variation.     

Retrospective analysis of Atlantic salmon (Salmo salar) marine growth and condition in the northwest Atlantic based on tag‐recovery data

The life history of North American Atlantic salmon (Salmo salar) is characterized by extensive round‐trip migrations between freshwater rearing habitats and marine feeding grounds off the coasts of Canada and Greenland. Growth is rapid during the marine migration, and growth rate and condition factor may be indicators of salmon health during this period. Growth data were evaluated from a tag‐recovery program conducted from 1969 to 1991 using hatchery‐reared Atlantic salmon smolts released in the Penobscot River, Maine, U.S.A. Information from recaptures of 3167 salmon that were at large in the marine environment for 1 month to 3 yr was analyzed. Length–weight measurements coupled with time‐at‐large data were used to estimate von Bertalanffy and allometric growth parameters specific to the marine phase. Variations in growth and condition factor in relation to smolt age, release date, and temperature conditions in the northwest Atlantic were also examined. The von Bertalanffy k parameter declined with ordinal release date, indicating faster growth rates during the first year of smolts released earlier in the spring. The 2‐yr‐old smolts had a larger k than 1‐yr‐old smolts, although 1‐yr‐old smolts grew to a larger asymptotic size. Sea surface temperature had variable effects on growth parameters and condition factor, with temperature at the beginning of the migration and in overwintering habitat during the first year at sea having the greatest influence on length–weight relationships. Determining the mechanisms that influence growth of individuals during the marine phase will help elucidate the factors responsible for historic growth trends, establishing a baseline for current research.     

Variation in wind and piscivorous predator fields affecting the survival of Atlantic salmon,Salmo salar,in the Gulf of Maine

Abstract Observations relevant to the North American stock complex of Atlantic salmon, Salmo salar L., suggest that marine mortality is influenced by variation in predation pressure affecting post‐smolts during the first months at sea. This hypothesis was tested for Gulf of Maine (GOM) stocks by examining wind pseudostress and the distribution of piscivorous predator fields potentially affecting post‐smolts. Marine survival has declined over recent decades with a change in the direction of spring winds, which is likely extending the migration of post‐smolts by favouring routes using the western GOM. In addition to changes in spring wind patterns, higher spring sea surface temperatures have been associated with shifting distributions of a range of fish species. The abundance of several pelagic piscivores, which based on their feeding habits may predate on salmon post‐smolts, has increased in the areas that serve as migration corridors for post‐smolts. In particular, populations of silver hake, Merluccius bilinearis (Mitchell), red hake, Urophycis chuss (Walbaum), and spiny dogfish, Squalus acanthias L., increased in size in the portion of the GOM used by post‐smolts. Climate variation and shifting predator distributions in the GOM are consistent with the predator hypothesis of recruitment control suggested for the stock complex.     

Competition between Asian pink salmon (Oncorhynchus gorbuscha) and Alaskan sockeye salmon (O. nerka) in the North Pacific Ocean

The importance of interspecific competition as a mechanism regulating population abundance in offshore marine communities is largely unknown. We evaluated offshore competition between Asian pink salmon and Bristol Bay (Alaska) sockeye salmon, which intermingle in the North Pacific Ocean and Bering Sea, using the unique biennial abundance cycle of Asian pink salmon from 1955 to 2000. Sockeye salmon growth during the second and third growing seasons at sea, as determined by scale measurements, declined significantly in odd‐numbered years, corresponding to years when Asian pink salmon are most abundant. Bristol Bay sockeye salmon do not interact with Asian pink salmon during their first summer and fall seasons and no difference in first year scale growth was detected. The interaction with odd‐year pink salmon led to significantly smaller size at age of adult sockeye salmon, especially among younger female salmon. Examination of sockeye salmon smolt to adult survival rates during 1977–97 indicated that smolts entering the ocean during even‐numbered years and interacting with abundant odd‐year pink salmon during the following year experienced 26% (age‐2 smolt) to 45% (age‐1 smolt) lower survival compared with smolts migrating during odd‐numbered years. Adult sockeye salmon returning to Bristol Bay from even‐year smolt migrations were 22% less abundant (reduced by 5.9 million fish per year) compared with returns from odd‐year migrations. The greatest reduction in adult returns occurred among adults spending 2 compared with 3 years at sea. Our new evidence for interspecific competition highlights the need for multispecies, international management of salmon production, including salmon released from hatcheries into the ocean.     

Growth, osmoregulation and sexual maturation of underyearling Atlantic salmon smolt Salmo salar L. exposed to different intensities of continuous light in sea cages

Atlantic salmon smolts are usually transferred to sea water during early spring, but photoperiod treatment can be used to produce underyearling (0+) smolts for transfer to sea water in late autumn, 7–8 months earlier than usual. This study investigated the effect of exposure to additional continuous light (LL) of different intensities on 0+ smolts after transfer to sea water. 0+ smolts transferred to sea cages in mid-October were exposed to natural light (NL) or LL of one of three intensities (low, medium or high) until January, whereupon they experienced NL until harvest in December. Fish in all groups displayed a normal ability to hypoosmoregulate, assessed by monitoring plasma chloride concentrations after transfer to sea water. No consistent differences in length, weight or condition were found between LL groups. The LL groups had greater growth in length than the NL group during the time of LL exposure, followed by an increase in weight when exposed to NL. This resulted in fish of larger size than the NL group. By August, the fish in the NL group had caught up with the LL groups in respect of length, weight and condition factors. This suggests that the LL treatment led to increased winter growth and phase-shifted a seasonal pattern of growth. The incidence of sexual maturation was low (< 1%), with no differences between groups.